| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28933091 | 0.882 | 0.160 | 1 | 156134474 | missense variant | C/A;G | snv | 4 | |||
| rs864622480 | 0.925 | 0.080 | 1 | 11998999 | missense variant | C/A;G | snv | 2 | |||
| rs56984562 | 0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv | 6 | |||
| rs57629361 | 0.827 | 0.280 | 1 | 156137207 | missense variant | C/A;G;T | snv | 9.3E-06 | 5 | ||
| rs863224968 | 1.000 | 0.080 | 1 | 12011547 | stop gained | C/A;G;T | snv | 1 | |||
| rs386134243 | 0.708 | 0.360 | 1 | 156135967 | missense variant | C/A;T | snv | 4.0E-06 | 16 | ||
| rs58596362 | 0.827 | 0.280 | 1 | 156138613 | splice region variant | C/A;T | snv | 8.1E-06 | 7 | ||
| rs267607561 | 1.000 | 0.080 | 1 | 156136240 | stop gained | C/A;T | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs267607623 | 1.000 | 0.080 | 1 | 156136021 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
| rs1557525153 | 1.000 | 0.080 | 1 | 11999031 | missense variant | C/G | snv | 1 | |||
| rs56793579 | 0.851 | 0.240 | 1 | 156115102 | missense variant | C/G;T | snv | 5 | |||
| rs121912496 | 0.882 | 0.120 | 1 | 156134910 | missense variant | C/G;T | snv | 3 | |||
| rs59914820 | 0.925 | 0.160 | 1 | 156115000 | missense variant | C/G;T | snv | 3 | |||
| rs267607620 | 0.925 | 0.120 | 1 | 156114929 | missense variant | C/G;T | snv | 6.0E-06 | 2 | ||
| rs119103262 | 1.000 | 0.080 | 1 | 11997315 | missense variant | C/G;T | snv | 1 | |||
| rs1340894696 | 1.000 | 0.080 | 1 | 156136083 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs267607617 | 1.000 | 0.080 | 1 | 156136027 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
| rs879254210 | 1.000 | 0.080 | 1 | 11998873 | stop gained | C/G;T | snv | 1 | |||
| rs119103263 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 19 | |||
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs58932704 | 0.776 | 0.200 | 1 | 156136413 | missense variant | C/T | snv | 8 | |||
| rs119103267 | 0.790 | 0.160 | 1 | 12009641 | missense variant | C/T | snv | 2.5E-04 | 2.8E-04 | 7 | |
| rs150840924 | 0.807 | 0.240 | 1 | 156136359 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 7 | |
| rs59026483 | 0.827 | 0.160 | 1 | 156134457 | missense variant | C/T | snv | 7.0E-06 | 7 | ||
| rs119103268 | 0.827 | 0.080 | 1 | 11992689 | missense variant | C/T | snv | 6 |